Angelman syndrome is a rare genetic disorder that approximately 500,000 people worldwide live with everyday. Like Gabriel, these individuals suffer from development delays, limited mobility, sleep disorders, and are nonverbal. Many have debilitating seizures. The disorder is caused by the silencing of one protein on the 15th chromosome. Scientists know that by activating that protein people living with Angelman syndrome can have a chance at a better quality of life. There are over 20 research partners working on a cure for Angelman syndrome. Please consider donating to Gabe’s fundraising page to support research, clinical trials, treatments, and potentially a cure.
Angelman Gabriel 